Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.747248
Title: NODAL/Activin signalling to chromatin : mechanisms of SMAD2-regulated transcription
Author: Coda, Davide Martino
ISNI:       0000 0004 7229 3068
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2018
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
NODAL/Activin signalling regulates key processes during embryonic development via SMAD2. How SMAD2 activates programmes of gene expression that are modulated over time, however, is not known. In this thesis, using the P19 embryonic teratoma cell line as a model system, I delineate the sequence of events that occur from SMAD2 binding to transcriptional activation, and the underlying mechanisms. I show that NODAL/Activin signalling induces dramatic changes in the chromatin landscape, and orchestrates a dynamic transcriptional network regulated by SMAD2, which acts via multiple mechanisms. By combining different genome-wide approaches, I have discovered two modes of SMAD2 binding. SMAD2 can bind pre-acetylated nucleosome-depleted sites, where it promotes a further increase in H3K9ac/H3K27ac. However, SMAD2 also binds to unacetylated, closed chromatin, independently of pioneer factors, where it induces nucleosome displacement and H3 acetylation. For a subset of genes, this requires cooperation with the remodeller SMARCA4 and the transcription factor FOXH1. I demonstrate that SMAD2 regulates RNA Polymerase II via de novo recruitment to target promoters, and that long term modulation of the transcriptional responses requires continued NODAL/Activin signalling. Moreover, SMAD2 binding does not necessarily equate with transcriptional kinetics, and my data suggest that SMAD2 recruits multiple co-factors during sustained signaling to shape the downstream transcriptional programme. I have used ATAC-seq to identify specific transcription factor footprints at SMAD2 binding sites, and future work will aim to unveil and characterise the network of transcription factors that collaborate with SMAD2 and enable cells to correctly interpret NODAL/Activin signaling over time.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.747248  DOI: Not available
Share: